Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		0.970 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0339537
Disease: Cone monochromatism
Cone monochromatism 		0.970 CausalMutation CLINVAR

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C3887980
Disease: Protanomaly
Protanomaly 		0.620 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0155015
Disease: Color Blindness, Red
Color Blindness, Red 		0.110 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0155015
Disease: Color Blindness, Red
Color Blindness, Red 		0.110 CausalMutation CLINVAR

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0009398
Disease: Color vision defect
Color vision defect 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0010036
Disease: Corneal dystrophy
Corneal dystrophy 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0027092
Disease: Myopia
Myopia 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0028738
Disease: Nystagmus
Nystagmus 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0085636
Disease: Photophobia
Photophobia 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0271388
Disease: Pendular Nystagmus
Pendular Nystagmus 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C3665347
Disease: Visual Impairment
Visual Impairment 		0.100 Biomarker HPO

Entrez Id: 5956
Gene Symbol: OPN1LW
OPN1LW
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		0.100 Biomarker HPO